Chaffey Benjamin T, Mitchell Elizabeth, Birch Mark A, Lakey Jeremy H
The Institute for Cell and Molecular Biosciences, The Medical School, Framlington Place, The University of Newcastle-upon-Tyne, Newcastle-upon-Tyne, Great Britain.
Int J Nanomedicine. 2008;3(3):287-93. doi: 10.2147/ijn.s2655.
Surface biology aims to observe and control biological processes by combining bio-, surface, and physical chemistry. Self-assembled monolayers (SAM) on gold surfaces have provided excellent methods for nanoscale surface preparation for such studies. However, extension of this work requires the specific immobilization of whole protein domains and the direct incorporation of recombinant proteins into SAM is still problematic. In this study a short random coil peptide has been designed to insert into thioalkane layers by formation of a hydrophobic helix. Surface plasmon resonance (SPR) studies show that specific immobilization via the internal cysteine is achieved. Addition of the peptide sequence to the terminus of a protein at the genetic level enables the production of a range of recombinant fusion-proteins with good yield. SPR shows that the proteins display the same gold-binding behavior as the peptide. It is shown that cell growth control can be achieved by printing the proteins using soft lithography with subsequent infilling with thio-alkanes The expression plasmid is constructed so that any stable protein domain can be easily cloned, expressed, purified and immobilized.
表面生物学旨在通过结合生物化学、表面化学和物理化学来观察和控制生物过程。金表面的自组装单分子层(SAM)为此类研究提供了出色的纳米级表面制备方法。然而,这项工作的扩展需要特定地固定整个蛋白质结构域,而将重组蛋白直接掺入SAM仍然存在问题。在本研究中,设计了一种短的无规卷曲肽,通过形成疏水螺旋插入硫代烷层。表面等离子体共振(SPR)研究表明,通过内部半胱氨酸实现了特异性固定。在基因水平上将肽序列添加到蛋白质末端能够高产率地生产一系列重组融合蛋白。SPR表明这些蛋白质表现出与肽相同的金结合行为。结果表明,通过使用软光刻技术印刷蛋白质并随后用硫代烷填充,可以实现细胞生长控制。构建表达质粒以便任何稳定的蛋白质结构域都能轻松克隆、表达、纯化和固定。